Regulation of Natural Cell Death in Dopaminergic Neurons of the Substantia Nigra by Striatal Glial Cell Line-Derived Neurotrophic Factor In Vivo
Dopamine (DA) neurons of the substantia nigra undergo a developmental cell death event that is biphasic, with peaks just after birth and at postnatal day 14. As envisioned by neurotrophic theory, this cell death is likely to be regulated by target interactions because it is augmented by their disrup...
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Veröffentlicht in: | The Journal of neuroscience 2003-06, Vol.23 (12), p.5141-5148 |
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description | Dopamine (DA) neurons of the substantia nigra undergo a developmental cell death event that is biphasic, with peaks just after birth and at postnatal day 14. As envisioned by neurotrophic theory, this cell death is likely to be regulated by target interactions because it is augmented by their disruption. However, the nature of the trophic molecules mediating this regulation are unknown. We showed in vitro that glial cell line-derived neurotrophic factor (GDNF) is able to suppress apoptotic death in DA neurons in postnatal primary culture. We now demonstrate in vivo that administration of GDNF into the striatal target is able to suppress apoptosis. Consistent with a possible physiologic role for endogenous striatal GDNF in regulating this event, two anti-GDNF neutralizing antibodies augment cell death. These antibodies augment cell death only during the first (immediately postnatal) phase of the biphasic death event. We conclude that GDNF is the leading candidate for a target-derived neurotrophic factor for the regulation of the early phase of natural cell death in DA neurons. |
doi_str_mv | 10.1523/jneurosci.23-12-05141.2003 |
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As envisioned by neurotrophic theory, this cell death is likely to be regulated by target interactions because it is augmented by their disruption. However, the nature of the trophic molecules mediating this regulation are unknown. We showed in vitro that glial cell line-derived neurotrophic factor (GDNF) is able to suppress apoptotic death in DA neurons in postnatal primary culture. We now demonstrate in vivo that administration of GDNF into the striatal target is able to suppress apoptosis. Consistent with a possible physiologic role for endogenous striatal GDNF in regulating this event, two anti-GDNF neutralizing antibodies augment cell death. These antibodies augment cell death only during the first (immediately postnatal) phase of the biphasic death event. We conclude that GDNF is the leading candidate for a target-derived neurotrophic factor for the regulation of the early phase of natural cell death in DA neurons.</description><identifier>ISSN: 0270-6474</identifier><identifier>ISSN: 1529-2401</identifier><identifier>EISSN: 1529-2401</identifier><identifier>DOI: 10.1523/jneurosci.23-12-05141.2003</identifier><identifier>PMID: 12832538</identifier><language>eng</language><publisher>United States: Soc Neuroscience</publisher><subject>Animals ; Animals, Newborn ; Antibodies - administration & dosage ; Antibody Specificity ; Apoptosis - drug effects ; Apoptosis - physiology ; Corpus Striatum - cytology ; Corpus Striatum - drug effects ; Corpus Striatum - metabolism ; Development/Plasticity/Repair ; Dopamine - metabolism ; Drug Administration Routes ; Glial Cell Line-Derived Neurotrophic Factor ; Nerve Growth Factors - administration & dosage ; Nerve Growth Factors - antagonists & inhibitors ; Nerve Growth Factors - physiology ; Neurons - cytology ; Neurons - drug effects ; Neurons - physiology ; Rats ; Rats, Sprague-Dawley ; Substantia Nigra - cytology ; Substantia Nigra - physiology</subject><ispartof>The Journal of neuroscience, 2003-06, Vol.23 (12), p.5141-5148</ispartof><rights>Copyright © 2003 Society for Neuroscience 0270-6474/03/235141-08.00/0 2003</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c433t-73c01d5acadcf1ae457b12e7c75979dafcb5eed8659256b60bc2293ec9c7a4e23</citedby><cites>FETCH-LOGICAL-c433t-73c01d5acadcf1ae457b12e7c75979dafcb5eed8659256b60bc2293ec9c7a4e23</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC6741204/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC6741204/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,314,727,780,784,885,27923,27924,53790,53792</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/12832538$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Oo, Tinmarla Frances</creatorcontrib><creatorcontrib>Kholodilov, Nikolai</creatorcontrib><creatorcontrib>Burke, Robert E</creatorcontrib><title>Regulation of Natural Cell Death in Dopaminergic Neurons of the Substantia Nigra by Striatal Glial Cell Line-Derived Neurotrophic Factor In Vivo</title><title>The Journal of neuroscience</title><addtitle>J Neurosci</addtitle><description>Dopamine (DA) neurons of the substantia nigra undergo a developmental cell death event that is biphasic, with peaks just after birth and at postnatal day 14. As envisioned by neurotrophic theory, this cell death is likely to be regulated by target interactions because it is augmented by their disruption. However, the nature of the trophic molecules mediating this regulation are unknown. We showed in vitro that glial cell line-derived neurotrophic factor (GDNF) is able to suppress apoptotic death in DA neurons in postnatal primary culture. We now demonstrate in vivo that administration of GDNF into the striatal target is able to suppress apoptosis. Consistent with a possible physiologic role for endogenous striatal GDNF in regulating this event, two anti-GDNF neutralizing antibodies augment cell death. These antibodies augment cell death only during the first (immediately postnatal) phase of the biphasic death event. We conclude that GDNF is the leading candidate for a target-derived neurotrophic factor for the regulation of the early phase of natural cell death in DA neurons.</description><subject>Animals</subject><subject>Animals, Newborn</subject><subject>Antibodies - administration & dosage</subject><subject>Antibody Specificity</subject><subject>Apoptosis - drug effects</subject><subject>Apoptosis - physiology</subject><subject>Corpus Striatum - cytology</subject><subject>Corpus Striatum - drug effects</subject><subject>Corpus Striatum - metabolism</subject><subject>Development/Plasticity/Repair</subject><subject>Dopamine - metabolism</subject><subject>Drug Administration Routes</subject><subject>Glial Cell Line-Derived Neurotrophic Factor</subject><subject>Nerve Growth Factors - administration & dosage</subject><subject>Nerve Growth Factors - antagonists & inhibitors</subject><subject>Nerve Growth Factors - physiology</subject><subject>Neurons - cytology</subject><subject>Neurons - drug effects</subject><subject>Neurons - physiology</subject><subject>Rats</subject><subject>Rats, Sprague-Dawley</subject><subject>Substantia Nigra - cytology</subject><subject>Substantia Nigra - physiology</subject><issn>0270-6474</issn><issn>1529-2401</issn><issn>1529-2401</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2003</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkV1v0zAUhiMEYmXwF5DFBVyl-CtxwwUSardRVHXSyri1HOek8ZTGne202r_gJ89ZytcVV5bl5zw-r94keUfwlGSUfbzroHfWazOlLCU0xRnhZEoxZs-SSSSKlHJMnicTTAVOcy74WfLK-zuMscBEvEzOCJ0xmrHZJPl5A9u-VcHYDtkarVXonWrRHNoWLUCFBpkOLexe7UwHbms0Wg-fd36gQwNo05c-qC4YhdZm6xQqH9AmOKNC1Fy15pdsFefTBThzgGp0BGf3TRReKh2sQ8sO_TAH-zp5UavWw5vTeZ7cXl58n39NV9dXy_mXVao5YyEVTGNSZUqrStdEAc9ESSgILbJCFJWqdZkBVLM8K2iWlzkuNaUFA11ooThQdp58Hr37vtxBpaELMbjcO7NT7kFaZeS_L51p5NYeZC44oZhHwfuTwNn7HnyQO-N1jKo6sL2XgnHKOSP_BcmsYKQgA_hpBHVs1zuof29DsByal9_WF7c315v5UsYLofKpeTk0H4ff_p3nz-ip6gh8GIHGbJujcSD9TrVtxIk8Ho-jcPCxR4GjvRc</recordid><startdate>20030615</startdate><enddate>20030615</enddate><creator>Oo, Tinmarla Frances</creator><creator>Kholodilov, Nikolai</creator><creator>Burke, Robert E</creator><general>Soc Neuroscience</general><general>Society for Neuroscience</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7TK</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20030615</creationdate><title>Regulation of Natural Cell Death in Dopaminergic Neurons of the Substantia Nigra by Striatal Glial Cell Line-Derived Neurotrophic Factor In Vivo</title><author>Oo, Tinmarla Frances ; Kholodilov, Nikolai ; Burke, Robert E</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c433t-73c01d5acadcf1ae457b12e7c75979dafcb5eed8659256b60bc2293ec9c7a4e23</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2003</creationdate><topic>Animals</topic><topic>Animals, Newborn</topic><topic>Antibodies - administration & dosage</topic><topic>Antibody Specificity</topic><topic>Apoptosis - drug effects</topic><topic>Apoptosis - physiology</topic><topic>Corpus Striatum - cytology</topic><topic>Corpus Striatum - drug effects</topic><topic>Corpus Striatum - metabolism</topic><topic>Development/Plasticity/Repair</topic><topic>Dopamine - metabolism</topic><topic>Drug Administration Routes</topic><topic>Glial Cell Line-Derived Neurotrophic Factor</topic><topic>Nerve Growth Factors - administration & dosage</topic><topic>Nerve Growth Factors - antagonists & inhibitors</topic><topic>Nerve Growth Factors - physiology</topic><topic>Neurons - cytology</topic><topic>Neurons - drug effects</topic><topic>Neurons - physiology</topic><topic>Rats</topic><topic>Rats, Sprague-Dawley</topic><topic>Substantia Nigra - cytology</topic><topic>Substantia Nigra - physiology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Oo, Tinmarla Frances</creatorcontrib><creatorcontrib>Kholodilov, Nikolai</creatorcontrib><creatorcontrib>Burke, Robert E</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Neurosciences Abstracts</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>The Journal of neuroscience</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Oo, Tinmarla Frances</au><au>Kholodilov, Nikolai</au><au>Burke, Robert E</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Regulation of Natural Cell Death in Dopaminergic Neurons of the Substantia Nigra by Striatal Glial Cell Line-Derived Neurotrophic Factor In Vivo</atitle><jtitle>The Journal of neuroscience</jtitle><addtitle>J Neurosci</addtitle><date>2003-06-15</date><risdate>2003</risdate><volume>23</volume><issue>12</issue><spage>5141</spage><epage>5148</epage><pages>5141-5148</pages><issn>0270-6474</issn><issn>1529-2401</issn><eissn>1529-2401</eissn><abstract>Dopamine (DA) neurons of the substantia nigra undergo a developmental cell death event that is biphasic, with peaks just after birth and at postnatal day 14. As envisioned by neurotrophic theory, this cell death is likely to be regulated by target interactions because it is augmented by their disruption. However, the nature of the trophic molecules mediating this regulation are unknown. We showed in vitro that glial cell line-derived neurotrophic factor (GDNF) is able to suppress apoptotic death in DA neurons in postnatal primary culture. We now demonstrate in vivo that administration of GDNF into the striatal target is able to suppress apoptosis. Consistent with a possible physiologic role for endogenous striatal GDNF in regulating this event, two anti-GDNF neutralizing antibodies augment cell death. These antibodies augment cell death only during the first (immediately postnatal) phase of the biphasic death event. We conclude that GDNF is the leading candidate for a target-derived neurotrophic factor for the regulation of the early phase of natural cell death in DA neurons.</abstract><cop>United States</cop><pub>Soc Neuroscience</pub><pmid>12832538</pmid><doi>10.1523/jneurosci.23-12-05141.2003</doi><tpages>8</tpages></addata></record> |
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subjects | Animals Animals, Newborn Antibodies - administration & dosage Antibody Specificity Apoptosis - drug effects Apoptosis - physiology Corpus Striatum - cytology Corpus Striatum - drug effects Corpus Striatum - metabolism Development/Plasticity/Repair Dopamine - metabolism Drug Administration Routes Glial Cell Line-Derived Neurotrophic Factor Nerve Growth Factors - administration & dosage Nerve Growth Factors - antagonists & inhibitors Nerve Growth Factors - physiology Neurons - cytology Neurons - drug effects Neurons - physiology Rats Rats, Sprague-Dawley Substantia Nigra - cytology Substantia Nigra - physiology |
title | Regulation of Natural Cell Death in Dopaminergic Neurons of the Substantia Nigra by Striatal Glial Cell Line-Derived Neurotrophic Factor In Vivo |
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